Radoslav I. Enchev

2.7k total citations · 1 hit paper
21 papers, 1.5k citations indexed

About

Radoslav I. Enchev is a scholar working on Molecular Biology, Cell Biology and Epidemiology. According to data from OpenAlex, Radoslav I. Enchev has authored 21 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 8 papers in Cell Biology and 4 papers in Epidemiology. Recurrent topics in Radoslav I. Enchev's work include Ubiquitin and proteasome pathways (14 papers), Autophagy in Disease and Therapy (4 papers) and Microtubule and mitosis dynamics (4 papers). Radoslav I. Enchev is often cited by papers focused on Ubiquitin and proteasome pathways (14 papers), Autophagy in Disease and Therapy (4 papers) and Microtubule and mitosis dynamics (4 papers). Radoslav I. Enchev collaborates with scholars based in United Kingdom, Switzerland and United States. Radoslav I. Enchev's co-authors include Matthias Peter, Brenda A. Schulman, Anne Schreiber, Edward P. Morris, da Fonseca, David Komander, Keith D. Wilkinson, Francisca E. Reyes‐Turcu, Yu Ye and Masato Akutsu and has published in prestigious journals such as Nature, Nature Communications and Nature Reviews Molecular Cell Biology.

In The Last Decade

Radoslav I. Enchev

20 papers receiving 1.5k citations

Hit Papers

Protein neddylation: beyo... 2014 2026 2018 2022 2014 100 200 300 400

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Radoslav I. Enchev United Kingdom 18 1.3k 295 292 249 127 21 1.5k
Jimi Wills United Kingdom 17 1.1k 0.8× 132 0.4× 423 1.4× 319 1.3× 61 0.5× 24 1.6k
Ivan Bosanac Canada 14 1.8k 1.3× 366 1.2× 346 1.2× 215 0.9× 272 2.1× 15 2.0k
Annette Flotho Germany 11 1.6k 1.2× 427 1.4× 352 1.2× 138 0.6× 185 1.5× 12 1.8k
Yusuke Sato Japan 27 1.6k 1.2× 431 1.5× 499 1.7× 294 1.2× 315 2.5× 58 2.0k
Marion Peter France 23 1.7k 1.3× 249 0.8× 740 2.5× 67 0.3× 87 0.7× 38 2.2k
Saskia Hutten Germany 21 2.5k 1.9× 208 0.7× 194 0.7× 105 0.4× 132 1.0× 31 2.9k
Georg Petzold Germany 16 2.0k 1.5× 539 1.8× 437 1.5× 100 0.4× 65 0.5× 19 2.2k
Anjanabha Saha United States 13 1.9k 1.4× 325 1.1× 155 0.5× 216 0.9× 78 0.6× 15 2.0k
Mary E. Matyskiela United States 19 1.7k 1.2× 450 1.5× 549 1.9× 300 1.2× 51 0.4× 21 1.8k
David Haselbach Austria 19 1.1k 0.8× 117 0.4× 284 1.0× 89 0.4× 65 0.5× 28 1.4k

Countries citing papers authored by Radoslav I. Enchev

Since Specialization
Citations

This map shows the geographic impact of Radoslav I. Enchev's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Radoslav I. Enchev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Radoslav I. Enchev more than expected).

Fields of papers citing papers by Radoslav I. Enchev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Radoslav I. Enchev. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Radoslav I. Enchev. The network helps show where Radoslav I. Enchev may publish in the future.

Co-authorship network of co-authors of Radoslav I. Enchev

This figure shows the co-authorship network connecting the top 25 collaborators of Radoslav I. Enchev. A scholar is included among the top collaborators of Radoslav I. Enchev based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Radoslav I. Enchev. Radoslav I. Enchev is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Nishimura, Shunsuke, Hidetaka Kioka, Shan Ding, et al.. (2025). HSC70 coordinates COP9 signalosome and SCF ubiquitin ligase activity to enable a prompt stress response. EMBO Reports. 26(5). 1344–1366. 1 indexed citations
2.
Maslen, Sarah, et al.. (2025). GroEL/ES chaperonin unfolds then encapsulates a nascent protein on the ribosome. Nature Communications. 16(1). 9976–9976.
3.
Clapperton, Julie A., Shan Ding, Simone Kunzelmann, et al.. (2023). Structural and mechanistic insights into the CAND1-mediated SCF substrate receptor exchange. Molecular Cell. 83(13). 2332–2346.e8. 14 indexed citations
4.
Enchev, Radoslav I., et al.. (2022). Structural dynamics: review of time-resolved cryo-EM. Acta Crystallographica Section D Structural Biology. 78(8). 927–935. 33 indexed citations
5.
Beláň, Ondrej, Consuelo Barroso, Artur Kaczmarczyk, et al.. (2021). Single-molecule analysis reveals cooperative stimulation of Rad51 filament nucleation and growth by mediator proteins. Molecular Cell. 81(5). 1058–1073.e7. 53 indexed citations
6.
Schreiber, Anne, Ben C. Collins, Colin Davis, et al.. (2021). Multilayered regulation of autophagy by the Atg1 kinase orchestrates spatial and temporal control of autophagosome formation. Molecular Cell. 81(24). 5066–5081.e10. 17 indexed citations
7.
Lee, Byungjin, Andrea Nans, Mohammad Mehdi Esfahani, et al.. (2020). Modular microfluidics enables kinetic insight from time-resolved cryo-EM. Nature Communications. 11(1). 3465–3465. 79 indexed citations
8.
Enchev, Radoslav I., Gili Ben‐Nissan, Yishai Levin, et al.. (2019). CSNAP, the smallest CSN subunit, modulates proteostasis through cullin-RING ubiquitin ligases. Cell Death and Differentiation. 27(3). 984–998. 19 indexed citations
9.
Gerez, Juan, Edward Rockenstein, U. Herrmann, et al.. (2019). A cullin-RING ubiquitin ligase targets exogenous α-synuclein and inhibits Lewy body–like pathology. Science Translational Medicine. 11(495). 32 indexed citations
10.
Cannavò, Elda, Sara N. Andres, Vera M. Kissling, et al.. (2018). Regulatory control of DNA end resection by Sae2 phosphorylation. Nature Communications. 9(1). 4016–4016. 60 indexed citations
11.
Ferretti, Lorenza P., Anika Trenner, Olga Murina, et al.. (2016). Cullin3-KLHL15 ubiquitin ligase mediates CtIP protein turnover to fine-tune DNA-end resection. Nature Communications. 7(1). 12628–12628. 55 indexed citations
12.
Courthéoux, Thibault, Radoslav I. Enchev, Fabienne Lampert, et al.. (2016). Cortical dynamics during cell motility are regulated by CRL3KLHL21 E3 ubiquitin ligase. Nature Communications. 7(1). 12810–12810. 26 indexed citations
13.
Reichermeier, Kurt M., Martin Winkler, Anne Schreiber, et al.. (2016). Structural and kinetic analysis of the COP9-Signalosome activation and the cullin-RING ubiquitin ligase deneddylation cycle. eLife. 5. 71 indexed citations
14.
Ulbricht, Anna, Christopher A. Barnes, Radoslav I. Enchev, et al.. (2016). A SPOPL/Cullin-3 ubiquitin ligase complex regulates endocytic trafficking by targeting EPS15 at endosomes. eLife. 5. e13841–e13841. 54 indexed citations
15.
Schumacher, Frances‐Rose, Keith Siew, Jinwei Zhang, et al.. (2015). Characterisation of the Cullin‐3 mutation that causes a severe form of familial hypertension and hyperkalaemia. EMBO Molecular Medicine. 7(10). 1285–1306. 82 indexed citations
16.
Birol, Melissa, Radoslav I. Enchev, André Padilla, et al.. (2014). Structural and Biochemical Characterization of the Cop9 Signalosome CSN5/CSN6 Heterodimer. PLoS ONE. 9(8). e105688–e105688. 27 indexed citations
17.
Enchev, Radoslav I., Brenda A. Schulman, & Matthias Peter. (2014). Protein neddylation: beyond cullin–RING ligases. Nature Reviews Molecular Cell Biology. 16(1). 30–44. 455 indexed citations breakdown →
18.
Enchev, Radoslav I., Daniel C. Scott, da Fonseca, et al.. (2012). Structural Basis for a Reciprocal Regulation between SCF and CSN. Cell Reports. 2(3). 616–627. 124 indexed citations
19.
Schreiber, Anne, Florian Stengel, Ziguo Zhang, et al.. (2011). Structural basis for the subunit assembly of the anaphase-promoting complex. Nature. 470(7333). 227–232. 137 indexed citations
20.
Enchev, Radoslav I., Anne Schreiber, Fabienne Beuron, & Edward P. Morris. (2010). Structural Insights into the COP9 Signalosome and Its Common Architecture with the 26S Proteasome Lid and eIF3. Structure. 18(4). 518–527. 60 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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